An uncommon complementary isochromosome of 46,XY, i(9)(p10), i(9)(q10) in an infertile oligoasthenoteratozoospermic man

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dc.contributor.authorGuven, Emine Seda Guvendag
dc.contributor.authorDilbaz, Serdar
dc.contributor.authorCeylaner, Serdar
dc.contributor.authorAcar, Hasan
dc.contributor.authorCinar, Ozgur
dc.contributor.authorOzdegirmenci, Ozlem
dc.contributor.authorKarcaaltincaba, Deniz
dc.date.accessioned2020-03-26T18:13:45Z
dc.date.available2020-03-26T18:13:45Z
dc.date.issued2011
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractObjective: To report a rare case of male infertility associated with oligoasthenoteratozoospermia and complementary isochromosome 46 XY, i(9)(p10), i(9)(q10). Design: Case report. Setting: Reference hospital. Patient(s): Infertile oligoastenozoospermic man with complementary isochromosome 46, XY, i(9)(p10), i(9)(q10). Intervention(s): Peripheral blood lymphocytes obtained for karyotyping, and florescence in situ hybridization (FISH) analysis for gonadal mosaicism in ejaculated spermatozoa. Main Outcome Measure(s): Physical examination, semen analysis, GBG banding, and FISH procedure. Result(s): The semen analysis revealed oligoasthenoteratozoospermia. The lymphocytic karyotype detected a complementary isochromosome 46, XY, i(9)(p10), i(9)(q10), and the FISH procedure showed abnormal sperm. Conclusion(s): This the first report of oligoasthenoteratozoospermia associated with complementary isochromosome 46, XY, i(9)(p10), i(9)(q10). (Fertil Steril (R) 2011;95:290.e5-e8. (C) 2011 by American Society for Reproductive Medicine.)en_US
dc.identifier.doi10.1016/j.fertnstert.2010.05.028en_US
dc.identifier.issn0015-0282en_US
dc.identifier.issn1556-5653en_US
dc.identifier.issue1en_US
dc.identifier.pmid20646692en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.urihttps://dx.doi.org/10.1016/j.fertnstert.2010.05.028
dc.identifier.urihttps://hdl.handle.net/20.500.12395/26127
dc.identifier.volume95en_US
dc.identifier.wosWOS:000285411600066en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherELSEVIER SCIENCE INCen_US
dc.relation.ispartofFERTILITY AND STERILITYen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectAzoospermiaen_US
dc.subjectisochromosomeen_US
dc.subjectmale infertilityen_US
dc.subjectnonrobertsonian translocationen_US
dc.titleAn uncommon complementary isochromosome of 46,XY, i(9)(p10), i(9)(q10) in an infertile oligoasthenoteratozoospermic manen_US
dc.typeEditorialen_US

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